Charité
Berlin, State of Berlin, 10117, Germany
NCT Number: NCT02358772
This is a comparison of clinical outcomes between a pre-hospital and an in-hospital thrombolysis patient registry.
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Notify Me18 year and older
All sexes
Observational
Berlin, State of Berlin, 10117, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: three months after event
dichotomized mRS 0-1 and 2-6 in patients who lived at home without assistance prior to the index stroke.
Time frame: three months after event
dichotomized mRS 1-3 and 4-6
Time frame: three months after event
mortality (mRS=6)
Time frame: three months after event
ordinal analysis across whole mRS range
Charite University, Berlin, Germany
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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